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CO5380014A1 - PHARMACEUTICAL FORMULATION FOR ORAL OR TOPIC ADMINISTRATION OF HYDROPHOBIC COMPOUNDS THAT DOES NOT FRAME EMULSION - Google Patents

PHARMACEUTICAL FORMULATION FOR ORAL OR TOPIC ADMINISTRATION OF HYDROPHOBIC COMPOUNDS THAT DOES NOT FRAME EMULSION

Info

Publication number
CO5380014A1
CO5380014A1 CO00061955A CO00061955A CO5380014A1 CO 5380014 A1 CO5380014 A1 CO 5380014A1 CO 00061955 A CO00061955 A CO 00061955A CO 00061955 A CO00061955 A CO 00061955A CO 5380014 A1 CO5380014 A1 CO 5380014A1
Authority
CO
Colombia
Prior art keywords
ch2or
chor
ch2o
fatty acids
oral
Prior art date
Application number
CO00061955A
Other languages
Spanish (es)
Inventor
Tomas Andrysek
Milan Stuchlik
Ales Vrana
Alexander Jegorov
Josef Stuchlik
Vladimir Matha
Original Assignee
Ivax Pharmaceuticals Sro
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10859192&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CO5380014(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Ivax Pharmaceuticals Sro filed Critical Ivax Pharmaceuticals Sro
Publication of CO5380014A1 publication Critical patent/CO5380014A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/12Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
    • A61K38/13Cyclosporins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/14Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0014Skin, i.e. galenical aspects of topical compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • A61K9/127Synthetic bilayered vehicles, e.g. liposomes or liposomes with cholesterol as the only non-phosphatidyl surfactant
    • A61K9/1274Non-vesicle bilayer structures, e.g. liquid crystals, tubules, cubic phases or cochleates; Sponge phases
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841Filling excipients; Inactive ingredients
    • A61K9/4858Organic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Dermatology (AREA)
  • Dispersion Chemistry (AREA)
  • Virology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Oncology (AREA)
  • Rheumatology (AREA)
  • AIDS & HIV (AREA)
  • Transplantation (AREA)
  • Pain & Pain Management (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Epoxy Compounds (AREA)

Abstract

Un método para incrementar la viscosidad de una formulación farmacéutica para administración oral o tópica que comprende los pasos de combinar:a) una cantidad efectiva de uno o más ingredientes activos hidrofobicos; b) de 5 a 50% de uno o más compuestos seleccionados de esteres de poliglicerol o ácidos grasos de fórmula (1) CH2OR-CHOR-CH2O-[CH2CHOR-CH2O-]NCH2-CHOR-CH2OR (1)en donde n es un entero de 4 a 13 y R es H ó CO RAND#39 en donde RAND#39 es un alquilo hidroxilado saturado o insaturado de C8-22 y en donde por lo menos un grupo R no es hidrógeno;c) de 5 a 50% de uno o más compuestos seleccionado de ésteres de poliglicerol o ácidos grasos y/o ácidos grasos insaturado de fórmula (2) CH2OR-CHOR-CH2O-[CH2CHOR-CH2O-]NCH2-CHOR-CH2OR (2)en donde N es un entero de 0 a 10 y R es H ó COR" en donde R" es un alquilo hidroxilado saturado o insaturado de C8-22, y en donde mientras al menos un grupo R no es hidrógeno;d) de 5 a 50% de uno o más compuestos seleccionados de triglicerido de macrogol ésteres de glicerol, gliceridos parciales o ácidos grasos ó esteres de macrogol de ácidos grasos en los cuales la cantidad promedio de oxido de etileno reaccionado en la síntesis de estas sustancias varia desde 50 a 150 moles y constantemente la proporción entre los componentes b) y d) es desde 0,1:1 hasta 10:1;en donde los anteriores porcentajes son seleccionados de un total del 100%;y donde después de la disolución con agua 1:1 en volumen la viscosidad de la disolución se incrementa hasta por lo menos 5 veces en comparación con la composición sin diluir.A method for increasing the viscosity of a pharmaceutical formulation for oral or topical administration comprising the steps of combining: a) an effective amount of one or more hydrophobic active ingredients; b) 5 to 50% of one or more compounds selected from polyglycerol esters or fatty acids of formula (1) CH2OR-CHOR-CH2O- [CH2CHOR-CH2O-] NCH2-CHOR-CH2OR (1) where n is a integer from 4 to 13 and R is H or CO RAND # 39 where RAND # 39 is a saturated or unsaturated hydroxylated alkyl of C8-22 and where at least one group R is not hydrogen; c) from 5 to 50% of one or more compounds selected from polyglycerol esters or fatty acids and / or unsaturated fatty acids of formula (2) CH2OR-CHOR-CH2O- [CH2CHOR-CH2O-] NCH2-CHOR-CH2OR (2) wherein N is an integer from 0 to 10 and R is H or COR "where R" is a saturated or unsaturated hydroxylated alkyl of C8-22, and where while at least one group R is not hydrogen; d) from 5 to 50% of one or more compounds selected from macrogol triglyceride glycerol esters, partial glycerides or fatty acids or fatty acid macrogol esters in which the average amount of ethylene oxide reacted in the synthesis of these substances s varies from 50 to 150 moles and constantly the ratio between components b) and d) is from 0.1: 1 to 10: 1; where the above percentages are selected from a total of 100%; and where after dissolution With 1: 1 volume water, the viscosity of the solution increases up to at least 5 times compared to the undiluted composition.

CO00061955A 1999-08-17 2000-08-17 PHARMACEUTICAL FORMULATION FOR ORAL OR TOPIC ADMINISTRATION OF HYDROPHOBIC COMPOUNDS THAT DOES NOT FRAME EMULSION CO5380014A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB9919288A GB2355656B (en) 1999-08-17 1999-08-17 Pharmaceutical compositions for oral and topical administration

Publications (1)

Publication Number Publication Date
CO5380014A1 true CO5380014A1 (en) 2004-03-31

Family

ID=10859192

Family Applications (1)

Application Number Title Priority Date Filing Date
CO00061955A CO5380014A1 (en) 1999-08-17 2000-08-17 PHARMACEUTICAL FORMULATION FOR ORAL OR TOPIC ADMINISTRATION OF HYDROPHOBIC COMPOUNDS THAT DOES NOT FRAME EMULSION

Country Status (40)

Country Link
US (1) US20070190132A1 (en)
EP (2) EP1334717B1 (en)
JP (2) JP2003507343A (en)
KR (2) KR100828748B1 (en)
CN (2) CN1382061A (en)
AR (2) AR025324A1 (en)
AT (2) ATE402691T1 (en)
AU (1) AU777740B2 (en)
BR (1) BR0013385A (en)
CA (2) CA2380951C (en)
CO (1) CO5380014A1 (en)
CY (1) CY1105318T1 (en)
CZ (2) CZ296591B6 (en)
DE (2) DE60018081T2 (en)
DK (2) DK1210119T3 (en)
EE (2) EE04955B1 (en)
EG (1) EG23994A (en)
ES (2) ES2237443T3 (en)
GB (1) GB2355656B (en)
HK (1) HK1049629A1 (en)
HR (1) HRP20020154B1 (en)
HU (1) HUP0203236A3 (en)
IL (4) IL148200A0 (en)
JO (1) JO2324B1 (en)
MX (1) MXPA02001631A (en)
NO (2) NO20020760L (en)
NZ (1) NZ517271A (en)
PE (1) PE20010636A1 (en)
PL (1) PL192769B1 (en)
PT (2) PT1210119E (en)
RU (2) RU2279894C2 (en)
SA (1) SA00210487B1 (en)
SG (1) SG143019A1 (en)
SI (1) SI1210119T1 (en)
SK (2) SK286083B6 (en)
TN (1) TNSN00173A1 (en)
UA (2) UA72539C2 (en)
UY (1) UY26303A1 (en)
WO (1) WO2001012229A1 (en)
ZA (2) ZA200308221B (en)

Families Citing this family (21)

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GB2355656B (en) * 1999-08-17 2004-04-07 Galena As Pharmaceutical compositions for oral and topical administration
FR2826261B1 (en) * 2001-06-26 2005-03-25 Lmd TOPICAL COMPOSITION COMPRISING A CYTOTOXIC PRODUCT AND ITS USE IN THE TREATMENT OF ALOPECHE
DE10154464B4 (en) * 2001-11-08 2005-10-20 Max Delbrueck Centrum Orally administrable pharmaceutical preparation comprising liposomally encapsulated taxol
KR20030065831A (en) * 2002-02-01 2003-08-09 주식회사 태평양 cyclosporin-containing sustained release pharmaceutical composition
US7101576B2 (en) * 2002-04-12 2006-09-05 Elan Pharma International Limited Nanoparticulate megestrol formulations
US9101540B2 (en) 2002-04-12 2015-08-11 Alkermes Pharma Ireland Limited Nanoparticulate megestrol formulations
EP1935407A1 (en) * 2002-12-03 2008-06-25 Elan Pharma International Limited Low viscosity liquid dosage forms
CN100337620C (en) * 2002-12-04 2007-09-19 日清药业股份有限公司 Water-soluble composition containing coenzyme q10
JP4518042B2 (en) * 2002-12-04 2010-08-04 日油株式会社 Method for producing water-soluble composition containing coenzyme Q10
KR20200083657A (en) * 2002-12-09 2020-07-08 아브락시스 바이오사이언스, 엘엘씨 Compositions and methods of delivery of pharmacological agents
US6979672B2 (en) * 2002-12-20 2005-12-27 Polichem, S.A. Cyclosporin-based pharmaceutical compositions
TW200616681A (en) * 2004-10-05 2006-06-01 Recordati Ireland Ltd Lercanidipine capsules
EP1806125B1 (en) * 2004-10-20 2011-08-03 Kao Corporation Liquid compositions for oral cavity
KR20080003322A (en) * 2005-02-24 2008-01-07 엘란 파마 인터내셔널 리미티드 Nanoparticle Blend of Docetaxel and Analogs thereof
WO2010060798A1 (en) * 2008-11-28 2010-06-03 Advance Holdings Limited Pharmaceutical formulation comprising diclofenac and a hydroxy fatty acid polyoxyalkylene ester
BRPI1008983A2 (en) * 2009-03-12 2016-03-22 Advance Holdings Ltd pharmaceutical formulation
KR101100933B1 (en) * 2009-04-23 2012-01-02 한국기술교육대학교 산학협력단 Solder ball remover
EP3274054A1 (en) 2015-03-27 2018-01-31 Arch Personal Care Products, L.P. Viscosity building composition for personal care products
CN112426403B (en) * 2020-12-09 2021-09-17 南京天纵易康生物科技股份有限公司 Oral ulcer gel and preparation method and application thereof
US20250186542A1 (en) * 2022-05-02 2025-06-12 Chugai Seiyaku Kabushiki Kaisha Composition containing peptide compound for use with surfactant
CN119770478B (en) * 2024-12-31 2025-12-19 美济生物医药(广州)有限公司 Paclitaxel oral pharmaceutical composition, preparation method and application thereof

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GB2222770B (en) * 1988-09-16 1992-07-29 Sandoz Ltd Pharmaceutical compositions containing cyclosporins
US6007840A (en) * 1988-09-16 1999-12-28 Novartis Ag Pharmaceutical compositions comprising cyclosporins
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CZ288631B6 (en) * 1996-01-18 2001-08-15 Galena, A. S. Therapeutic preparations containing cyclosporin
CZ288739B6 (en) * 1996-08-01 2001-08-15 Galena, A. S. Cyclosporin containing medicinal preparations
CZ267796A3 (en) * 1996-09-12 1998-04-15 Galena A.S. Medicamentous preparations, particularly for internal application in the form of inherently micro-emulsifying therapeutical systems
EP0973502A1 (en) * 1997-03-12 2000-01-26 Abbott Laboratories Lipophilic binary systems for the administration of lipophilic compounds
DK0969856T3 (en) * 1997-03-12 2005-05-02 Abbott Lab Hydrophilic binary systems for the administration of cyclosporine
AU728698B2 (en) * 1997-07-29 2001-01-18 Boehringer Ingelheim International Gmbh Self-emulsifying formulation for lipophilic compounds
US6063762A (en) * 1997-12-05 2000-05-16 Chong Kun Dang Corp. Cyclosporin-containing microemulsion preconcentrate composition
US20030216303A1 (en) * 1998-03-06 2003-11-20 Michael Ambuhl Emulsion preconcentrates containing cyclosporin or a macrolide
GB2355656B (en) * 1999-08-17 2004-04-07 Galena As Pharmaceutical compositions for oral and topical administration

Also Published As

Publication number Publication date
IL148200A0 (en) 2002-09-12
DE60322454D1 (en) 2008-09-11
IL148200A (en) 2007-12-03
AR025324A1 (en) 2002-11-20
ZA200201315B (en) 2004-06-30
CZ2002575A3 (en) 2003-05-14
PT1334717E (en) 2008-10-09
SA00210487B1 (en) 2006-09-10
GB9919288D0 (en) 1999-10-20
BR0013385A (en) 2002-05-07
CA2380951A1 (en) 2001-02-22
ATE288766T1 (en) 2005-02-15
EP1210119A1 (en) 2002-06-05
RU2279894C2 (en) 2006-07-20
JO2324B1 (en) 2005-09-12
DE60018081D1 (en) 2005-03-17
HK1049629A1 (en) 2003-05-23
CN101406453A (en) 2009-04-15
EG23994A (en) 2008-03-10
HRP20020154B1 (en) 2006-07-31
CA2380951C (en) 2010-03-23
UY26303A1 (en) 2001-03-16
MXPA02001631A (en) 2003-07-14
DK1334717T3 (en) 2008-11-24
EE04954B1 (en) 2008-02-15
IL158108A (en) 2010-04-15
NO20020760L (en) 2002-04-16
PT1210119E (en) 2005-05-31
AU777740B2 (en) 2004-10-28
SK286083B6 (en) 2008-03-05
UA72539C2 (en) 2005-03-15
SI1210119T1 (en) 2005-06-30
CZ296170B6 (en) 2006-01-11
SK2482002A3 (en) 2002-12-03
US20070190132A1 (en) 2007-08-16
NO20034778L (en) 2002-04-16
JP2003507343A (en) 2003-02-25
EP1334717A3 (en) 2004-01-02
EE04955B1 (en) 2008-02-15
EE200200075A (en) 2003-04-15
NO20020760D0 (en) 2002-02-15
DE60018081T2 (en) 2006-01-05
PL192769B1 (en) 2006-12-29
JP2004238399A (en) 2004-08-26
DK1210119T3 (en) 2005-06-20
KR20020059367A (en) 2002-07-12
GB2355656A (en) 2001-05-02
KR100828747B1 (en) 2008-05-09
SG143019A1 (en) 2008-06-27
TNSN00173A1 (en) 2005-11-10
UA75926C2 (en) 2006-06-15
PE20010636A1 (en) 2001-06-02
AU6461300A (en) 2001-03-13
ATE402691T1 (en) 2008-08-15
EP1210119B1 (en) 2005-02-09
CZ296591B6 (en) 2006-04-12
ES2311077T3 (en) 2009-02-01
ZA200308221B (en) 2004-09-29
NO20034778D0 (en) 2003-10-24
ES2237443T3 (en) 2005-08-01
RU2279895C2 (en) 2006-07-20
HUP0203236A3 (en) 2004-06-28
CA2452118A1 (en) 2001-02-22
PL353445A1 (en) 2003-11-17
RU2003133451A (en) 2005-04-20
EP1334717A2 (en) 2003-08-13
CN1382061A (en) 2002-11-27
HRP20020154A2 (en) 2003-12-31
CY1105318T1 (en) 2010-03-03
WO2001012229A1 (en) 2001-02-22
KR20050095651A (en) 2005-09-29
IL158108A0 (en) 2004-03-28
HUP0203236A2 (en) 2003-01-28
GB2355656B (en) 2004-04-07
AR043106A2 (en) 2005-07-20
KR100828748B1 (en) 2008-05-09
EP1334717B1 (en) 2008-07-30
EE200300371A (en) 2003-10-15
NZ517271A (en) 2004-02-27

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